Donald Corenman MD DC | Spine Surgeon Colorado

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Viewing 4 posts - 1 through 4 (of 4 total)

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Kipper
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January 24, 2014 at 4:03 am

Post count: 5

in reply to: Fusion failure after 10.5 yrs? #10215

Hi Dr. Corenman,

I wanted to update you on this whole mess. I’ve had a CT and flexion/extension Xray done. The fusions are intact based on those (thank you LORD).

There is a herniation at C4-5.

Pain has settled and become localized but intense in the neck with occasional twinges to the right upper arm (and I do mean occasional). The neurosurgeon told me that if this was my first rodeo he’d definitely do a fusion. Because this is my third go-round, he does not want to do that. I’m 43, already have C5-6-7 fused, have somewhat limited ROM as it is…so he referred me to physical therapy and pain management. I will see him again at the end of February.

I’ve had several sessions of PT. I started even though I could not get into the pain clinic for a month (now two weeks away). I’m sort of regretting that decision because I end up in huge pain following these sessions, and for the following day also. The sessions are very painful but I have a high tolerance for pain. Unfortunately I’m still not getting sleep because the neck hurts so darn much.

I’m very reluctant (make that steadfastly against) having an ESI. Petrified is not too strong a word. The neurosurgeon told me they don’t twilight you or anything when they do this, just use local. I frankly do not think I can even bear that thought. Also, from what I understand they use some kind of contrast (is this correct?) and I have a history of anaphylactic reactions to various IV contrasts. That scares me a lot, too.

Is my fear completely irrational? I’m not sure exactly what I’m afraid of. I know at my first appointment they aren’t going to stick a needle in my neck, and really all I want is some kind of systemic painkiller just to get me through the nights. I’m about stir crazy with lack of sleep. I don’t want to “kick the can down the road” if the ESI would just be a temporary relief. The DPT I’m seeing is confident my pain will be reduced with continuing PT (I do have significantly more motion in my neck after only 2 weeks) but so far the pain is constant and sometimes worse than before I started PT. Again, the movement improvement is awesome, but I don’t really care if I can look a few more degrees to the right or left when it hurts so much all the time.

The neurosurgeon mentioned another type of surgery that might help, and for the life of me I can’t think of the name of it. He just really doesn’t want to fuse another level. I’m glad he’s conservative. I just wish I didn’t have so much darn PAIN.

Thank you in advance for your opinion on whether or not I’m nuts. ;)

Kipper
Member

December 17, 2013 at 1:46 am

Post count: 5

in reply to: Fusion failure after 10.5 yrs? #9964

You have certainly helped me feel better. I’ll come back after I get the CT/X-ray result (and/or whatever records I can lay my hands on) and let you know what’s going on. I don’t even care if my head falls off at this point, if I could just get rid of the pain.

Kipper
Member

December 16, 2013 at 10:23 pm

Post count: 5

in reply to: Fusion failure after 10.5 yrs? #9960

Oh thank you! I don’t know why I didn’t think to call the hospital; I’ll be doing that today. And thank you for the shoulder/neck information. It’s definitely not the shoulder/thoracic outlet syndrome by those two indicators.

I am still trying to get over the idea that there isn’t a fusion where there’s supposed to be a fusion.

Hypothetically…if the graft has dissolved, (which it would have had to have done in the last 6.5 years since the second surgery, since they surely would have noticed that, right?), other than the pain I’m having, is there a danger to not doing anything about it?

Kipper
Member

December 16, 2013 at 8:22 pm

Post count: 5

in reply to: Fusion failure after 10.5 yrs? #9958

Thank you so much for replying to me!!! I very much appreciate it. I know the first one was done with an autograft…I have the dent in my hip to prove it. :) That’s another reason I find it so bizarre!

After reading your very informative response along with parts of your site, I’m starting to think I did a poor job explaining my pain to the neurosurgeon. I admit that I have been pretty upset about this, and with the lack of sleep and pain I’m not really “myself”. I guess there’s not a whole lot I can do until I have the Xray and CT and return to him in January.

I’m way out of my element. When the first incident happened, I had a dozen referrals to the surgeon I went to. I did everything he told me to do and beyond (from acupuncture to PT to pain management) and did end up having the surgery. He told me that there were “protein strands” irritating the nerves, describing the disc as “shredded” (at the C5-6 level). The second time, I actually had thought I’d hurt my shoulder. I went directly to PT, and it was there that it was determined it was not my shoulder at all, but my neck. Back to the neurosurgeon and before I could blink, I was having the second level fused. The recovery from that one was easier because of the allograft.

I’ve been trying to get the records from the first two procedures so at least we have something to go by. I’m having zero luck with that, unfortunately (keep leaving messages at the practice, keep getting no call back…I’m sending in a written request today and hoping for the best).

The hand pain comes in little “zaps” to the thumb side of the hand, palm side. The forearm pain and tricep-area pain also comes in zaps. (By “zaps” I mean it’s not constant, and when it comes it feels, well, “zappy”.) It is not an unbroken “line” of pain. I feel it in my neck primarily (and I do mean primarily…it is constant there, but has zaps or “waves” of more intensity).

I wonder if this is all in my head. :(
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Viewing 4 posts - 1 through 4 (of 4 total)

Donald Corenman, MD, DC

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81 reviews

Eric S

Sep 26, 2021

by Eric S on Donald Corenman, MD, DC

Successful pars repair at 46 years old

Back in November of 2018 (at 46 years old) I came from Vancouver BC to have a pars repair done with Dr. Donald Corenman at the Steadman Clinic in Vail Colorado. I'm finally posting this review nearly three years later in late 2021. The reason I waited so long was I wanted to know the final result before I posted my review. Unfortunately in that time Dr. Corenman has retired. Nevertheless, I want to post this review of Dr. Corenman and his staff at the Steadman Clinic in their excellent treatment of my L5 pars interarticularis.

I fractured my pars at age 42 back in 2014 when rolling on the gym floor, and was denied treatment by the Canadian healthcare system, probably due to my age. First my GP told me there was no surgical option for a pars defect, which was quite incorrect! I tried to live with it, but the symptoms worsened (periodic random spine slippage and weeks of resultant pain after just bending over to tie my shoe, so I eventually learned to mostly squat and hardly bend). When I finally consulted with Canadian spine surgeons, I was told they believed my pars defect had been congenital (since birth). This was absurd, considering I had done extreme martial arts (including jiu jitsu) for years prior, as well as 5 years of reinforcing steel full time in my 20s, probably the hardest job on the back you can find. No pars defect like mine would possibly have allowed this--ergo it was impossible that I had had the defect since birth. I did however have an asymptomatic congenital spina bifida occulta that made me more susceptible to a pars fracture. In 2014 in one instant, I went from having the strongest back people I knew said they'd ever seen, to being unable to safely bend over and tie my shoe without a non-negligible risk of my spine slipping randomly (which would lead to weeks of pain after each occurrence). This was due to the unilateral L5 pars defect, otherwise known as spondylolysis. It was when lying in pain on the floor 4 years later after maybe the 6th spine slippage event post injury, that I had had enough, and resolved to have surgery. If Canada's "universal health care" said no, I would make lemonade from lemons, and find the very best surgeon in the world at pars repairs. That was Dr. Donald Corenman. Dr. Corenman back in 2018 ran a website https://neckandback.com/ that dedicated many pages to the science of every aspect of pars repairs, from eligibility (good discs on MRI), to best surgical techniques (minimal open compared to minimally invasive), best imaging to use (i.e., O-Arm with Stealth imaging vs. older fluoroscopy), the ideal amount of BMP to use and why not use too much or too little, and much more, all to do with pars repairs, pages upon pages of his site just on the pars, with scientific references and his own extensive expert opinion. As a health research statistician, I was very impressed with this. It was in stark contrast to the websites of other spine surgeons which barely gave the pars a word or two, focusing almost exclusively on fusions. I had found the best surgeon in the world for pars repairs, and so after Dr. Corenman personally screened my MRI to ensure my discs were healthy, I booked the surgery.

Being 46 years old at the time of surgery in 2018, with a 4-year-old pars fracture from 2014 combined with a congenital SBO meant my pars fragment was somewhat atrophied, but it was "very solid", said Dr. Corenman in the operative report. Nevertheless, it was challenging with two things to fix, the pars and SBO, and OR time was around 4 hours. Recovery over the following months was guided by a very clear "Spine binder" from the Steadman Clinic with strict rules of "no BLT" (no bending, lifting or twisting), and illustrated physiotherapy guidelines. They even warned patients to avoid fish oil supplements, which could excessively dampen inflammation and hence slow bone healing. They answered many questions I had during months of recovery, with responses coming from the very supportive Lori Fugate (then director of Dr. Corenman's practice), and Ehrich Bean (then physician's assistant at the practice), as well as a couple calls with Dr. Corenman himself after two of the CT scans. Ehrich Bean offered great advice for taking the spine binder conservatively due to the nature of pars repairs vs. fusions. The final post-op CT scan I had was a couple weeks ago at 34 months post-op, and Dr. Corenman had retired, but I got a very positive and informative call from Eric Strauch (current PA at the Steadman Clinic under Dr. Corenman's replacement there, and who had also worked with Dr. Corenman previously). The staff at the Steadman Clinic were extremely supportive all the way through the process. I should mention, the local Canadian spine surgeon did offer me very good post-operative support including antibiotics as needed to deal with a mild surface incision-site infection early on, booking numerous x-rays when I felt something was amiss, as well as booking all four of my post-op CT scans. I am very grateful for that support also.

My final result shows plenty of solid bone across the pars and a healed SBO, with my vertebral body now a solid bone ring instead of being broken at two places as it was pre-op. Does my spine hold up in the real world? You bet! I have recently dug and moved several yards of dirt and sand and gravel by myself (shovel and wheelbarrow!) to fix our water main, pulled roots from the yard, moved several "portable" (these are HUGE) air conditioners up several flights of stairs my myself, and lifted weights. I now run 2 miles (3.2 KM) several times weekly with a hard 100 meter dash in the middle. I bend deeply before each run I go on, with no spine slippage. My spine feels amazing. I can bend over to do exercise, or real word tasks, with no risk of spine slippage.

My sincere thanks to God, Dr. Donald Corenman, Lori Fugate, Ehrich Bean, Eric Strauch, and the Steadman Clinic, as well as the Canadian spine surgeon who offered me excellent post-operative care back in Canada. You have all given me a new lease on life.

Sincerely,
Eric S

Robert S

May 11, 2021

by Robert S on Donald Corenman, MD, DC

Back Fusion Surgery

I had my entire lumbar spine fused in November of 2018. I had scoliosis , with pinched nerves that were so painful I could hardly walk - and standing for more than a few minutes was impossible. Even sitting was painful.
The fusion surgery produced immediate relief! And the recovery was much easier than I expected.
To this day I can do all the activities I love from hiking, to standing in a stream fly fishing to riding my bike long distances - or just walking down the street with my wife.
Kudos to Dr. Corenman and his staff, (including the two Erics) for taking such good care of me!

Leslie R

Jul 9, 2020

by Leslie R on Donald Corenman, MD, DC

TLIF

I had my TLIF surgery on 6/24/2020 by Dr. Corenman, I can not say enough good things about the Dr or his staff. I was always treated with respect and explained everything throughly, that made it easy for everyone to understand. I highly recommend Dr. Corenman and the Steadman Clinic.

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Kipper

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